FDA Inspection 555705 — Stericycle Inc

Stericycle Inc — FEI 3007097064

The FDA completed an inspection of Stericycle Inc on January 12, 2009 in Bannockburn, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 12, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Bannockburn, IL (United States)